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Tesamorelin: Research, Handling and Batch Documentation

Tesamorelin is GHRH(1-44) carrying a trans-3-hexenoyl group on its N-terminal tyrosine, an analogue that acts at the GHRH receptor.

Part of Volta's peptides.

Identity and specification

Form
Lyophilized powder
Appearance
White lyophilised powder
Other known names
TH9507
Compound class
GHRH analogue (GHRH receptor agonist)
CAS number
218949-48-5
Molecular formula
C₂₂₃H₃₇₀N₇₂O₆₉S
Molecular weight
5,195.9 g/mol
PubChem CID
44147413
Production
Synthetic, by solid-phase peptide synthesis
Solubility
Soluble in sterile water
Shelf life
24 months from date of manufacture

Molecular structure, sequence and the published laboratory studies on Tesamorelin are in the compound library entry for Tesamorelin.

Vial sizes available

Every size of Tesamorelin Volta lists, in stock or not. Each is a separate catalogue page with its own batch number and specification table.

Purity and batch documentation

Volta's release specification is >99% (HPLC). That is a threshold we set. >99% is the specification every batch is released to. The figure on a certificate is what a laboratory measured for one lot.

Research on Tesamorelin

Handling and stability

Regulatory context

Tesamorelin in Canada

Tesamorelin is authorized in Canada only as a prescription drug product. What Volta supplies is research material, not that product, and the two are not interchangeable.

  • Health Canada has authorized tesamorelin as a prescription drug product, which carries a Drug Identification Number (DIN). Research material is not that product and carries no DIN.
  • An approved drug product carries a DIN, a monograph, a specified formulation and a manufacturer accountable for it. Research material carries a certificate of analysis for identity and purity and nothing else.
  • Volta supplies tesamorelin for in-vitro laboratory research only. It is not the authorized drug product, is not dispensed against a prescription, and is not authorised for human use.
Is tesamorelin approved in Canada?
Only as a specific prescription drug product authorized by Health Canada. That authorization covers that drug product, not tesamorelin supplied as research material.
Is research-grade tesamorelin the same as the authorized drug product?
No. The authorized drug product has a DIN, a published monograph and a specified formulation. Research material is supplied against a certificate of analysis for identity and purity, is not manufactured to a drug product specification, and is for in-vitro laboratory use only.
Why is tesamorelin supplied as research material if an approved product exists?
The approved product is a medicine, supplied through pharmacies against a prescription. Laboratory research on the molecule is a separate activity that needs the compound itself rather than a finished drug product, which is what research-grade material is for.
Does Volta's tesamorelin have a Health Canada DIN?
No. A DIN belongs to an authorized drug product, and research material is not one. Any research-grade peptide presented as carrying a DIN is misrepresented.

Regulatory position verified 2026-10-10. Positions change; this page states the date it was last checked rather than implying it is current.

More peptides

Tesamorelin sits in Volta's peptides group, alongside the other compounds of the same composition. The whole range is on the full research catalogue, and the library of comparisons and guides is under peptide research.

Research use only. For in-vitro laboratory research by qualified professionals only. Not for human or animal administration. Not a drug, food, cosmetic or dietary supplement. Not intended to diagnose, treat, cure, mitigate or prevent any disease. Volta does not provide dosing, administration or protocol guidance for any material listed. Read the full research disclaimer.

Cluster last reviewed: 2026-09-15.

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